Compound heterozygosity of a novel exon 3 frameshift (p.R357P fs*24) mutation and Y486D mutation in exon 5 of the UGT1A1 gene in a Thai infant with Crigler-Najjar syndrome type 2.
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| Description | scientific article published on 13 April 2015 |
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author: Yong Poovorawan |
| Publication date | April 13, 2015 |
| Language | English |
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